Protective effect of diphenylmethyl selenocyanate against CCl4-induced hepatic injury

被引:16
作者
Das, Rajat Kumar [1 ]
Hossain, Sk. Ugir [1 ]
Bhattacharya, Sudin [1 ]
机构
[1] Chittaranjan Natl Canc Inst, Dept Canc Chemoprevent, Kolkata 700026, W Bengal, India
关键词
organoselenocyanates; diphenylmethyl selenocyanate; carbon tetrachloride (CCl4); CCl4 induced liver necrosis; CCl4 induced liver apoptosis; CCl4 induced DNA damage; comet assay;
D O I
10.1002/jat.1230
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Organoselenocyanates represent an important class of chemopreventive agent, which possess antioxidative, antimutagenic as well as cancer chemopreventive properties. The present study is an attempt to evaluate the protective effect of diphenylmethyl selenocyanate - a synthetic organoselenocyanate against carbon tetrachloride (CCl4)-induced hepatic damage in Swiss albino mice in vivo. Mice were pretreated with the Se-compound orally in a duration dependent manner (7 and 15 days) to observe its protective action against an acute toxic dose (24 h) of CCl4 (single injection at a dose of 20 mu l and 50 mu l kg(-1) b.w.) that induced hepatic necrosis and caused DNA damage (strand breaks) in the hepatocytes. This study revealed that pretreatment with the Se-compound reduced the extent of massive hepatic necrosis in a duration dependent manner, but it had no modulatory effect on hepatocellular apoptosis caused by acute toxic doses of CCl4. It was also found that the Se-compound could significantly (P < 0.01) prevent the CCl4-induced elevation of DNA damage in hepatocytes measured by comet assay in a duration dependent manner. So these findings will further strengthen the view that organoselenocyanate is an effective chemopreventive agent against acute hepatic damage, caused by halogenated alkanes such as CCl4. Copyright (C) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:527 / 537
页数:11
相关论文
共 48 条
[1]   Centrilobular endothelial cell injury by diquat in the selenium-deficient rat liver [J].
Atkinson, JB ;
Hill, KE ;
Burk, RF .
LABORATORY INVESTIGATION, 2001, 81 (02) :193-200
[2]   CCL4-INDUCED TOXICITY IN ISOLATED HEPATOCYTES - THE IMPORTANCE OF DIRECT SOLVENT INJURY [J].
BERGER, ML ;
BHATT, H ;
COMBES, B ;
ESTABROOK, RW .
HEPATOLOGY, 1986, 6 (01) :36-45
[3]  
Boll M, 2001, Z NATURFORSCH C, V56, P649
[4]  
Boll M, 2001, Z NATURFORSCH C, V56, P111
[5]   Protective effect of diphenyl diselenide on acute liver damage induced by 2-nitropropane in rats [J].
Borges, LP ;
Borges, VC ;
Moro, AV ;
Nogueira, CW ;
Rocha, JBT ;
Zeni, G .
TOXICOLOGY, 2005, 210 (01) :1-8
[6]   Effects of black tea, green tea and wine extracts on intestinal carcinogenesis induced by azoxymethane in F344 rats [J].
Caderni, G ;
De Filippo, C ;
Luceri, C ;
Salvadori, M ;
Giannini, A ;
Biggeri, A ;
Remy, S ;
Cheynier, V ;
Dolara, P .
CARCINOGENESIS, 2000, 21 (11) :1965-1969
[7]   DIRECT ENZYMATIC DETECTION OF ENDOGENOUS OXIDATIVE BASE DAMAGE IN HUMAN LYMPHOCYTE DNA [J].
COLLINS, AR ;
DUTHIE, SJ ;
DOBSON, VL .
CARCINOGENESIS, 1993, 14 (09) :1733-1735
[8]   APOPTOSIS - MOLECULAR CONTROL POINT IN TOXICITY [J].
CORCORAN, GB ;
FIX, L ;
JONES, DP ;
MOSLEN, MT ;
NICOTERA, P ;
OBERHAMMER, FA ;
BUTTYAN, R .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1994, 128 (02) :169-181
[9]   PREVENTION OF CARBON TETRACHLORIDE-INDUCED RAT-LIVER INJURY BY SOLUBLE TUMOR-NECROSIS-FACTOR RECEPTOR [J].
CZAJA, MJ ;
XU, J ;
ALT, E .
GASTROENTEROLOGY, 1995, 108 (06) :1849-1854
[10]  
Das Rajat Kumar, 2004, Asian Pac J Cancer Prev, V5, P151